ClinVar Miner

List of variants in gene CYP1B1 reported as uncertain significance for anterior segment dysgenesis

Included ClinVar conditions (34):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 109
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HGVS dbSNP gnomAD frequency
NM_000104.4(CYP1B1):c.*1027del rs144188082 0.00927
NM_000104.4(CYP1B1):c.241T>A (p.Tyr81Asn) rs9282671 0.00362
NM_000104.4(CYP1B1):c.*981T>C rs9341262 0.00358
NM_000104.4(CYP1B1):c.-2G>A rs9341245 0.00309
NM_000104.4(CYP1B1):c.*1062G>T rs185371002 0.00297
NM_000104.4(CYP1B1):c.*2333G>A rs35320531 0.00263
NM_000104.4(CYP1B1):c.*2349G>A rs9341268 0.00257
NM_000104.4(CYP1B1):c.*3024T>C rs532039339 0.00257
NM_000104.4(CYP1B1):c.*2207G>A rs9341267 0.00244
NM_000104.4(CYP1B1):c.*118C>G rs1799885 0.00226
NM_000104.4(CYP1B1):c.*1460A>G rs137915099 0.00198
NM_000104.4(CYP1B1):c.147C>A (p.Ser49=) rs4987137 0.00191
NM_000104.4(CYP1B1):c.-84T>C rs886055999 0.00139
NM_000104.4(CYP1B1):c.*1056G>C rs187540802 0.00137
NM_000104.4(CYP1B1):c.*380G>A rs35007750 0.00137
NM_000104.4(CYP1B1):c.1103G>A (p.Arg368His) rs79204362 0.00125
NM_000104.4(CYP1B1):c.1078T>C (p.Leu360=) rs141245683 0.00121
NM_000104.4(CYP1B1):c.*466G>A rs9341260 0.00116
NM_000104.4(CYP1B1):c.*1938G>A rs570132783 0.00085
NM_000104.4(CYP1B1):c.*1075G>C rs77105857 0.00054
NM_000104.4(CYP1B1):c.*1746T>C rs34169771 0.00053
NM_000104.4(CYP1B1):c.*115G>A rs555706078 0.00046
NM_000104.4(CYP1B1):c.*1781T>C rs750990195 0.00035
NM_000104.4(CYP1B1):c.*1005C>T rs35978993 0.00033
NM_000104.4(CYP1B1):c.155C>T (p.Pro52Leu) rs201824781 0.00030
NM_000104.4(CYP1B1):c.*1683A>G rs189809220 0.00029
NM_000104.4(CYP1B1):c.*2760C>A rs375588205 0.00021
NM_000104.4(CYP1B1):c.*1798T>G rs900163227 0.00019
NM_000104.4(CYP1B1):c.182G>A (p.Gly61Glu) rs28936700 0.00017
NM_000104.4(CYP1B1):c.850C>T (p.Arg284Trp) rs368249322 0.00015
NM_000104.4(CYP1B1):c.1089C>T (p.Val363=) rs148461905 0.00014
NM_000104.4(CYP1B1):c.*1269T>A rs570388762 0.00013
NM_000104.4(CYP1B1):c.1168C>T (p.Arg390Cys) rs148542782 0.00013
NM_000104.4(CYP1B1):c.1033C>T (p.Leu345Phe) rs66583685 0.00012
NM_000104.4(CYP1B1):c.*1141A>G rs759611970 0.00011
NM_000104.4(CYP1B1):c.*917G>A rs3755026 0.00011
NM_000104.4(CYP1B1):c.319C>G (p.Leu107Val) rs56339482 0.00011
NM_000104.4(CYP1B1):c.592G>A (p.Val198Ile) rs59472972 0.00009
NM_000104.4(CYP1B1):c.*233A>G rs9341259 0.00008
NM_000104.4(CYP1B1):c.-80C>G rs894434388 0.00008
NM_000104.4(CYP1B1):c.859G>A (p.Ala287Thr) rs201544164 0.00008
NM_000104.4(CYP1B1):c.226C>A (p.Arg76Ser) rs377210850 0.00007
NM_000104.4(CYP1B1):c.701C>T (p.Thr234Met) rs375391843 0.00007
NM_000104.4(CYP1B1):c.711G>T (p.Ala237=) rs780375338 0.00007
NM_000104.4(CYP1B1):c.*1491G>T rs562799717 0.00006
NM_000104.4(CYP1B1):c.653A>T (p.Asp218Val) rs72549383 0.00006
NM_000104.4(CYP1B1):c.*2597A>G rs746236755 0.00005
NM_000104.4(CYP1B1):c.1047T>C (p.Tyr349=) rs775908245 0.00005
NM_000104.4(CYP1B1):c.*1346A>G rs960122791 0.00004
NM_000104.4(CYP1B1):c.*2209A>G rs949462503 0.00004
NM_000104.4(CYP1B1):c.*2499T>C rs886055988 0.00004
NM_000104.4(CYP1B1):c.367T>C (p.Phe123Leu) rs769402060 0.00004
NM_000104.4(CYP1B1):c.431A>G (p.Gln144Arg) rs753847648 0.00004
NM_000104.4(CYP1B1):c.918G>A (p.Gly306=) rs748708268 0.00004
NM_000104.4(CYP1B1):c.*105C>T rs756083290 0.00003
NM_000104.4(CYP1B1):c.*1561A>C rs34474461 0.00003
NM_000104.4(CYP1B1):c.8C>A (p.Thr3Asn) rs372685881 0.00003
NM_000104.4(CYP1B1):c.947A>T (p.Asp316Val) rs749521942 0.00003
NM_000104.4(CYP1B1):c.*1173del rs3834137 0.00002
NM_000104.4(CYP1B1):c.*1611G>A rs572531079 0.00002
NM_000104.4(CYP1B1):c.-1-10C>T rs780269033 0.00002
NM_000104.4(CYP1B1):c.*1079C>G rs886055994 0.00001
NM_000104.4(CYP1B1):c.*1601C>T rs886055992 0.00001
NM_000104.4(CYP1B1):c.*1730A>G rs886055991 0.00001
NM_000104.4(CYP1B1):c.*1895C>T rs886055990 0.00001
NM_000104.4(CYP1B1):c.*1910A>G rs1405956907 0.00001
NM_000104.4(CYP1B1):c.*1956A>G rs1235898139 0.00001
NM_000104.4(CYP1B1):c.*2151T>C rs886055989 0.00001
NM_000104.4(CYP1B1):c.*2498T>C rs572548236 0.00001
NM_000104.4(CYP1B1):c.*3086T>A rs969140341 0.00001
NM_000104.4(CYP1B1):c.*43C>T rs371252753 0.00001
NM_000104.4(CYP1B1):c.*661T>A rs886055995 0.00001
NM_000104.4(CYP1B1):c.1202A>G (p.His401Arg) rs886055997 0.00001
NM_000104.4(CYP1B1):c.1474G>A (p.Asp492Asn) rs776848093 0.00001
NM_000104.4(CYP1B1):c.24C>T (p.Asn8=) rs142995558 0.00001
NM_000104.4(CYP1B1):c.277C>T (p.Pro93Ser) rs1156997078 0.00001
NM_000104.4(CYP1B1):c.381C>T (p.Ser127=) rs780857657 0.00001
NM_000104.4(CYP1B1):c.498C>G (p.Leu166=) rs775055418 0.00001
NM_000104.4(CYP1B1):c.503G>A (p.Gly168Asp) rs200724605 0.00001
NM_000104.4(CYP1B1):c.763C>T (p.Arg255Cys) rs886055998 0.00001
NM_000104.4(CYP1B1):c.985G>A (p.Gly329Ser) rs777678299 0.00001
NM_000104.4(CYP1B1):c.*1450T>C rs886055993
NM_000104.4(CYP1B1):c.*1544G>A rs1682376790
NM_000104.4(CYP1B1):c.*1766G>A rs1682371906
NM_000104.4(CYP1B1):c.*1908G>A rs34544682
NM_000104.4(CYP1B1):c.*1961G>C rs767403314
NM_000104.4(CYP1B1):c.*2289G>T rs1682355981
NM_000104.4(CYP1B1):c.*2304A>C rs909259463
NM_000104.4(CYP1B1):c.*2314dup rs561615550
NM_000104.4(CYP1B1):c.*2660T>A rs886055987
NM_000104.4(CYP1B1):c.*3064A>T rs1682335231
NM_000104.4(CYP1B1):c.*3078G>A rs886055986
NM_000104.4(CYP1B1):c.*493G>A rs886055996
NM_000104.4(CYP1B1):c.*688T>C rs1682396717
NM_000104.4(CYP1B1):c.*864T>C rs987237179
NM_000104.4(CYP1B1):c.*867dup rs200949126
NM_000104.4(CYP1B1):c.*879del rs4646433
NM_000104.4(CYP1B1):c.*945C>T rs1327335898
NM_000104.4(CYP1B1):c.*972T>C rs1682390062
NM_000104.4(CYP1B1):c.*980A>C rs34521017
NM_000104.4(CYP1B1):c.-197C>G rs886056001
NM_000104.4(CYP1B1):c.1590T>C (p.Asp530=) rs146770394
NM_000104.4(CYP1B1):c.1593T>G (p.Ser531Arg) rs901961745
NM_000104.4(CYP1B1):c.371G>A (p.Arg124His) rs1177366364
NM_000104.4(CYP1B1):c.644G>C (p.Ser215Thr) rs72549384
NM_000104.4(CYP1B1):c.712G>T (p.Gly238Cys) rs1682493984
NM_000104.4(CYP1B1):c.809A>G (p.Asn270Ser) rs1381317977
NM_000104.4(CYP1B1):c.92C>A (p.Ala31Asp)
NM_000104.4(CYP1B1):c.958G>T (p.Val320Leu) rs72549382

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